Library / Laws / 119th Congress / House Bills / H.R. 6117
H.R. 6117
To amend the Federal Food, Drug, and Cosmetic Act to authorize requiring the manufacturers of a covered device to disclose to a patient all patient-specific data that is recorded or transmitted by the device and accessible to the manufacturer, and for other purposes.
| Print stage | Date | Size | ⠃ |
|---|---|---|---|
| Introduced in House | 2025-11-18 | 4.7K | ⠃⠗⠋ |